FDA Drug recall D-0340-2019
Oxybutynin Chloride Tablets, USP, 5 mg, 500-count bottle, Rx only, Mfd
- FDA Drug
- Class II
- terminated
- Published 2018-12-26
On 2018-12-26 the FDA classified a Class II recall of Oxybutynin Chloride Tablets, USP, 5 mg, 500-count bottle, Rx only, Mfd by Kvk Tech, citing labeling: Wrong bar code.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0340-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-12-11 |
| Published | 2018-12-26 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | Kvk Tech |
| Distribution | US |
Product
Oxybutynin Chloride Tablets, USP, 5 mg, 500-count bottle, Rx only, Mfd. By: KVK-Tech, Inc., Newtown, PA 18940, NDC 10702-201-50
Reason
Labeling: Wrong bar code
Identifiers
| ndc | 10702-201-01 |
|---|---|
| ndc | 10702-201-50 |
| ndc | 10702-201-10 |
| code_info | Lot #: 15079A, Exp 10/20 |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0340-2019%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.